INFLUENCE OF RATE OF ADMINISTRATION OF RACLOPRIDE ON AKATHISIA AND PROLACTIN RESPONSE

被引:3
作者
MOVINOSSWALD, G
KARLSSON, P
HAMMARLUNDUDENAES, M
FARDE, L
机构
[1] KAROLINSKA HOSP,DEPT PSYCHIAT & PSYCHOL,S-10401 STOCKHOLM,SWEDEN
[2] UPPSALA UNIV,DEPT BIOPHARMACEUT & PHARMACOKINET,S-75123 UPPSALA,SWEDEN
关键词
AKATHISIA; PROLACTIN; MAN; RACLOPRIDE; RATE OF ADMINISTRATION;
D O I
10.1007/BF02244845
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The D-2-dopamine receptor antagonist raclopride was administered to eight healthy male subjects, who had previously experienced akathisia following antipsychotic drugs. The influence of administration rate on onset, severity and duration of akathisia and on prolactin response was studied. Raclopride 3, 5 or 9 mg or placebo (P) was administered as single IV infusions during 10 min (R10 min/3 mg), 1 h (R1h/5 mg) or 4 h (R4h/9 mg) according to a randomized double-blind design. Despite a 24-fold difference in administration rate a similar peak raclopride concentration of about 350 nmol/1 was obtained after all three infusions. Three of the eight subjects experienced akathisia following R10 min/3 mg and R1h/5 mg, respectively. After R4h/9 mg seven subjects experienced akathisia of longer duration but not more severe than after the short infusions. The incidence and duration of akathisia seem to be mainly related to the plasma raclopride concentrations over time, whereas the rate of administration might be more important for the severity. A maximal prolactin response was induced which was not markedly affected by the rate of administration.
引用
收藏
页码:248 / 256
页数:9
相关论文
共 16 条
[1]   NEUROLEPTIC-INDUCED AKATHISIA - A REVIEW [J].
ADLER, LA ;
ANGRIST, B ;
REITER, S ;
ROTROSEN, J .
PSYCHOPHARMACOLOGY, 1989, 97 (01) :1-11
[2]   A RATING-SCALE FOR DRUG-INDUCED AKATHISIA [J].
BARNES, TRE .
BRITISH JOURNAL OF PSYCHIATRY, 1989, 154 :672-676
[3]  
FARDE L, 1988, ARCH GEN PSYCHIAT, V45, P71
[4]   AN OPEN LABEL TRIAL OF RACLOPRIDE IN ACUTE SCHIZOPHRENIA - CONFIRMATION OF D2-DOPAMINE RECEPTOR OCCUPANCY BY PET [J].
FARDE, L ;
WIESEL, FA ;
JANSSON, P ;
UPPFELDT, G ;
WAHLEN, A ;
SEDVALL, G .
PSYCHOPHARMACOLOGY, 1988, 94 (01) :1-7
[5]   QUANTITATIVE-ANALYSIS OF D2 DOPAMINE RECEPTOR-BINDING IN THE LIVING HUMAN-BRAIN BY PET [J].
FARDE, L ;
HALL, H ;
EHRIN, E ;
SEDVALL, G .
SCIENCE, 1986, 231 (4735) :258-261
[6]  
FARDE L, 1992, ARCH GEN PSYCHIAT, V49, P538
[7]   SELECTIVE D1-DOPAMINE AND D2-DOPAMINE RECEPTOR BLOCKADE BOTH INDUCES AKATHISIA IN HUMANS - A PET STUDY WITH [C-11] SCH-23390 AND [C-11] RACLOPRIDE [J].
FARDE, L .
PSYCHOPHARMACOLOGY, 1992, 107 (01) :23-29
[8]   THE NEW SELECTIVE D2-DOPAMINE RECEPTOR ANTAGONIST RACLOPRIDE - PHARMACOKINETICS, SAFETY AND TOLERABILITY IN HEALTHY-MALES [J].
FARDE, L ;
VONBAHR, C ;
WAHLEN, A ;
NILSSON, L ;
WIDMAN, M .
INTERNATIONAL CLINICAL PSYCHOPHARMACOLOGY, 1989, 4 (02) :115-126
[9]  
Gibaldi M., 1982, PHARMACOKINETICS
[10]   SPECIFIC INVITRO AND INVIVO BINDING OF H-3-RACLOPRIDE - A POTENT SUBSTITUTED BENZAMIDE DRUG WITH HIGH-AFFINITY FOR DOPAMINE D-2 RECEPTORS IN THE RAT-BRAIN [J].
KOHLER, C ;
HALL, H ;
OGREN, SO ;
GAWELL, L .
BIOCHEMICAL PHARMACOLOGY, 1985, 34 (13) :2251-2259